AuCl3-Catalyzed Hemiacetal Activation for the Stereoselective Synthesis of 2-Deoxy Trehalose Derivatives

A new practical, catalytic, and highly stereoselective method for directly accessing 1,1-α,α′-linked 2-deoxy trehalose analogues via AuCl3-catalyzed dehydrative glycosylation using hemiacetal glycosyl donors and acceptors is described. The method relies on the chemoselective Brønsted acid-type activation of tribenzylated 2-deoxy hemiacetals in the presence of other less reactive hemiacetals.

A ccessing structurally defined carbohydrates is essential to probe the complex biological roles that carbohydrates play. 1,2 Thus, the development of novel, efficient, and practical strategies for the stereoselective formation of glycosidic linkages, to add to the existing toolkit of carbohydrate chemistry, is still needed to push the boundaries of glycobiology research. 3− 6 Trehalose is a symmetrical disaccharide composed of two 1,1-α,α′-linked glucose subunits. Trehalose monomycolate (TMM) and dimycolate (TDM), bearing one and two 6-Omycolyl substituents, respectively, are produced in all mycobacterial species and have been shown to be crucial components of the outer layer of the cell wall of Mycobacterium tuberculosis (Mtb). These glycolipids play essential roles in Mtb cell wall biosynthesis and in the viability and virulence of the pathogen. 2,7,8 Targeting trehalose uptake and subsequent metabolism has garnered attention in recent years as an attractive route for the development of novel therapeutics and diagnostic agents. 9−14 Previous elegant studies reported the synthesis of a series of symmetrical and unsymmetrical trehalose mimetics, including amino, azido, fluoro, iodo, 2deoxy, and phosphate functionalities, as well as a fluoresceinfunctionalized analogue that was shown to label Mtb. 10 Subsequently, a range of differently functionalized trehalose analogues with fluorescent dyes 12,15,16 and biorthogonal handles, 17 including azides, 18,19 alkynes, 11,20 and photoactivatable diazirines, 21 have been shown to be metabolically incorporated into the mycomembrane of live mycobacteria. Different strategies exist by which unsymmetrical, functionalized trehalose derivatives can be accessed. 22,23 Enzymatic methods have been successfully applied to the synthesis of a range of trehalose analogues. 24,25 Alternatively, chemical synthesis involving either the desymmetrization of natural trehalose or chemical glycosylation of two separate building blocks is also possible. The former often requires long regioselective protection/deprotection and functional group interconversion sequences with the desymmetrisation step often being low-yielding. 26 On the contrary, chemical glycosylation can be used for the construction of the 1,1α,α′-linkage, bringing together a glycosyl donor and a hemiacetal acceptor; however, unlike enzymatic syntheses, the chemical synthesis of unsymmetrical trehalose derivatives is often more problematic due to the potential for the formation of up to four diastereomers, unwanted dimerization of the reactive components, and the formation of side products, decreasing the efficiency of the overall synthesis. Alternative methods for the stereoselective synthesis of unsymmetrical α,α′-linked trehalose derivatives using intramolecular aglycone delivery have been described. 27,28 Moreover, the synthesis of ketoside-type analogues of trehalose via Lewis acid-catalyzed activation of exoglycals and ketoside hemiacetals has also been reported. 29 Our group is interested in the development of expedient and efficient catalytic methods for the synthesis of 2-deoxy glycosides, which are prominent components of a number of natural products. 4 A number of glycosylation protocols exist for the stereoselective formation of 2-deoxy linkages, 4 but few examples of 2-deoxy trehalose analogues have been reported. For instance, symmetrical 2-deoxy trehalose derivatives via debenzylation deiodination of a 2,2′-diiodo derivative prepared by dehydrative dimerization of the benzylated 2-iodo hemiacetal have been described. 30 McGarrigle et al. reported the organocatalytic synthesis of symmetrical and unsymmetrical 2deoxy trehalose derivatives via activation of galactal 1; unfortunately, the products were formed as a mixture of anomers. 31 Herein, we report the development of a new, practical, and stereoselective method for accessing 1,1-α,α′linked 2-deoxy trehalose derivatives via AuCl 3 -catalyzed dehydrative glycosylation using hemiacetal glycosyl donors and acceptors.
During our previous work on the synthesis of 2-deoxy glycosides via the Au(I)/Ag(I)-catalyzed activation of glycals, we found that activation of 1 using Lewis acidic AuCl 3 formed an inseparable mixture of products, including 2,3-unsaturated Ferrier products (Scheme 1, top). 32 As part of our ongoing work on the development of catalytic glycosylation methods, AuCl 3 was further investigated as a catalyst for the activation of 2-deoxy hemiacetals 2a 33 and 3a 34 as an alternative starting material to the 1,2-unsaturated glycals.
Gold catalysis has been widely applied to carbohydrate synthesis. 35 For instance, AuCl 3 has been reported for the catalytic activation of acetylated glycals to give 2,3-unsaturated Ferrier products, 36 thioglycosides, 37 trichloroacetimidates, 38 and alkynyl donors. 39,40 AuBr 3 has also been reported for the activation of methyl glycosides. 41 Moreover, a number of methods for the activation of glycosyl hemiacetals using Lewis and Brønsted acids have been reported for the activation of glycosyl hemiacetals, 4,5 including gold chloride in combination with allyl trimethylsilane to generate C-glycosides. 42 However, to the best of our knowledge, the application of AuCl 3 for the direct activation of hemiacetals to access O-glycosides has not been reported to date.
In our initial studies, we found 1 mol % AuCl 3 in EtOAc at 50°C could catalyze the glycosylation of tribenzylated 2-deoxy galactosyl hemiacetal 2a with 4a to give the corresponding 2deoxy galactoside 5a in 70% yield with an α:β ratio of 12:1 (Table 1, entry 1). Following these encouraging results, hemiacetals 2a−c and 3a were reacted with a range of primary nucleophiles using between 1 and 3 mol % AuCl 3 in either EtOAc or toluene to form the corresponding 2-deoxy glycosides in 59−84% yields. In all cases, the α-anomer was favored (α:β = 3.3:1 to >15:1) ( Table 1, entries 1−9). See the Supporting Information for full details and solvent and temperature optimization screening. 43 Lower yields (10− Scheme 1. AuCl 3 -Catalyzed Activation of 2-Deoxy Hemiacetals Generally, glycosylation reactions are conducted under strictly anhydrous conditions to minimize unwanted hydrolysis of the glycosyl donor. In our case, performing the AuCl 3catalyzed reactions under an inert atmosphere or using anhydrous solvents did not have an effect on the reaction yield or time, demonstrating that the process is compatible with the use of "wet" solvents and can be performed under air. Dimerization of the hemiacetal donors was detected when secondary alcohols were used as acceptors in the Au(III)catalyzed reactions, which suggested the reaction condition could be amenable to the direct synthesis of 2,2′-deoxy trehalose mimetics. To that end, hemiacetal donors 2a or 3a were treated with 1 mol % AuCl 3 in toluene in the absence of any alternative OH nucleophile. Pleasingly, dimers 10 and 11 were isolated in 55% yields. In both cases, only the α,α′-linked products were observed (Scheme 2). Reaction of 6-deoxy fucose hemiacetal 9 44 under the same conditions led to the formation of 12 in 60% yield (only the α,α′-linked). When less reactive donors 2b, 2c, and 3b were employed, no reaction was observed, suggesting the substrates are unreactive toward glycosylation and dimerization under the mild conditions. 45 The difference in reactivity of the functionalized hemiacetals under our reaction conditions paved the way for the investigation of the selective activation of more reactive 2deoxy hemiacetals (e.g., 2a and 3a) as a method for providing access to unsymmetrical trehalose derivatives. To this end, differently protected hemiacetal acceptors 13a−c, 14, and 2c were reacted with 2a, 3a, and 2d using 2.5 mol % AuCl 3 in toluene at 50°C, and the desired unsymmetrical products 15a−g, 16, and 17a−c were isolated in 32−76% yields and exclusively as α,α′-linked products (Table 2). 46 Hemiacetal 2d protected with an acetate group at O-6 was also synthesized and successfully glycosylated with acceptor 13a to form disaccharide 16 in 54% yield (entry 4). 47 One of the advantages of this chemoselective strategy is the ability to perform orthogonal late-stage functionalizations. To exemplify this, the divergent synthesis of 6-azido derivatives 21 and 25 from common disaccharide 17c was carried out (Scheme 3). Selective deprotection of the benzyl or benzoyl protecting groups could be performed using palladiummediated hydrogenolysis in 95% yield or LiOH-mediated ester hydrolysis (98% yield), respectively. In each case, a tosyl group was selectively installed at the more reactive O-6 hydroxyl group. In the case of 19, NaN 3 treatment gave 6-azido disaccharide 20. Following ester hydrolysis, 6-azido trehalose derivative 21 was accessed with the azido group installed on the 2-deoxyglucose unit. Due to the instability of azido groups to common reductive methods, 6-tosyl disaccharide 23 was

Organic Letters pubs.acs.org/OrgLett
Letter hydrogenated in the presence of palladium to form 24, and the 6-tosyl group was then converted into an azido group to give 25, whereby the glucose unit bears the 6-azido group. Mechanistically, it was initially postulated that AuCl 3 could act as a Lewis acid, coordinating to the hydroxyl group of the 2-deoxy hemiacetal to promote the formation of a transient oxocarbenium ion that can react with the less reactive hemiacetal acceptor. However, we found addition of organic or inorganic bases (DIPEA or K 2 CO 3 ) stopped the reaction (Scheme S1), indicating a Brønsted acid-type mechanism might be plausible. 48 It was also found that dimerization of 2deoxy hemiacetal donor 2a also occurred upon treatment with HCl, albeit in lower yields (Table S6). However, formation of unsymmetrical trehalose derivative 15e using benzoylated hemiacetal 2a and acceptor 13c was not observed using HCl (Scheme S2). A number of different activation conditions were also tested for this reaction, but lower yields and/or less clean reaction profiles were observed compared to those with the use of AuCl 3 (Table S7). 1 H NMR spectroscopy studies in d 8toluene with equimolar mixtures of AuCl 3 and hemiacetal acceptor 13c did not indicate any interaction or reaction between the gold catalyst and the nucleophile ( Figure S1). Although it cannot be entirely ruled out as a reactive intermediate, 2-deoxy glycosyl chlorides were not observed at any point by NMR spectroscopy. Moreover, a 4:1 α,α′/α,β′anomeric mixture of 15b 31 was subjected to the reaction conditions using 2.5 mol % AuCl 3 to investigate whether the α,α′ selectivity was the result of in situ anomerization. An increase in the proportion of the α,β′ diastereomer as well as the formation of small amounts of hydrolyzed hemiacetal 13a was observed (Table S5). These results indicate the α,α′ selectivity of the reaction is not due to anomerization and highlights the importance of not leaving the reactions for longer than necessary.
In summary, we have developed a new practical and catalytic method for the synthesis of 2-deoxy trehalose derivatives via Au(III) chemoselective activation of tribenzylated 2-deoxy hemiacetals in the presence of other less reactive hemiacetals.
Due to the catalytic nature of the activation system, the glycosylation reactions could be performed under nonanhydrous conditions. Despite starting with a mixture of anomers for both the donor and the acceptor, only the α,α′linked products were generated. The protecting group pattern of the acceptors could be varied, and this allows for the orthogonal modification of functionality at a later stage. The versatility of this approach was highlighted via the synthesis of 6-and 6′-azido-functionalized 2-deoxy trehalose analogues, which are useful tools for studying the biosynthetic pathway of Mtb.